A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947763



Internal ID18594610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21027697..21030987hg38UCSC Ensembl
Innerchr10:21316626..21319916hg19UCSC Ensembl
Innerchr10:21356632..21359922hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383291
hg193291
hg183291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1835559, nssv1835565, nssv1832581, nssv1835558, nssv1835563, nssv1835560, nssv1835562, nssv1835564, nssv1835561, nssv1832580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNEBL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947763
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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